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366 results about "Hydroxyapatite composite" patented technology

Preparation method of grapheme/hydroxyapatite composite material

A preparation method of a grapheme/hydroxyapatite composite material comprises the following steps: uniformly mixing oxidized grapheme with the concentration of 0.5-5 mg/ml and a solution or a turbid liquid with the calcium ion concentration of 0.01-3.0 mol/L to obtain a first mixed solution; adding a solution I with the phosphate anion concentration of 0.01-2.0 mol/L to the first mixed solution according to the molar ratio of calcium to phosphorus is (1.5-2.0) to 1, and uniformly mixing the solution I and the first mixed solution under the action of magnetic mixing; adjusting the pH to be 8-14 through a pH adjusting agent to obtain a second mixed solution; transferring the second mixed solution to a reaction kettle; carrying out hydro-thermal treatment for 1-12 hours at the temperature of 160-240 DEG C; cooling the second mixed solution until the temperature of the second mixed solution is the room temperature; cleaning, freezing and drying to obtain the grapheme/hydroxyapatite composite material. The preparation method is environment-friendly, simple and beneficial to large-scale production. The prepared grapheme/hydroxyapatite composite material has the advantages of good mechanical property as well as high electrical conductivity, adsorbability, biocompatibility and osteogenic activity.
Owner:SOUTHWEST JIAOTONG UNIV

Collagen/hydroxyapatite composite artificial bone and preparation method thereof

The invention relates to a collagen/hydroxyapatite composite artificial bone and a preparation method thereof. The artificial bone comprises type I collagen, hydroxyapatite and poly-p-dioxanone. The preparation method disclosed by the invention comprises the following steps: adding the type I collagen in a solvent to prepare a collagen solution, adding an appropriate amount of the hydroxyapatite and performing uniform stirring; placing the mixed slurry in a mold, performing pre-freezing, performing freeze-dried forming, and crushing the freeze-dried forming porous material to obtain blended powder; dissolving the poly-p-dioxanone in tetrafluoroacetic acid to prepare a solution, adding the blended powder in proportion, performing uniform stirring and performing cold press forming; and washing the formed pre-product with water, and drying the washed pre-product to obtain collagen/hydroxyapatite composite artificial bone. The preparation method disclosed by the invention is simple and low in the production cost. The collagen/hydroxyapatite composite artificial bone has compressive strength of 75-90MPa and favorable toughness, so that the collagen/hydroxyapatite composite artificial bone can meet requirements for bone filling and partial replacement in orthopedic surgery.
Owner:WUHAN YIJIABAO BIOMATERIAL CO LTD

Method for preparing bioactive poly(lactic-co-glycolic acid)/collagen/hydroxyapatite composite fiber membrane for bone repair

The invention discloses a method for preparing a bioactive poly (lactic-co-glycolic acid)/collagen/hydroxyapatite composite fiber membrane for bone repair. The method comprises the following steps of: treating a poly (lactic-co-glycolic acid) electrospun nanofiber membrane by using plasma, coating collagen, and immersing the poly (lactic-co-glycolic acid) electrospun nanofiber membrane into a simulated human physiologic body fluid to mineralize to obtain the poly (lactic-co-glycolic acid)/collagen/hydroxyapatite composite fiber membrane. The preparation method of the invention has the advantages of simpleness, high speed and wide material sources. By adopting the method of plasma treatment and coating, the highly-bionic nanofiber composite membrane is prepared by the steps of introducing collagen with osteocyte epimatrix into the poly (lactic-co-glycolic acid) electrospun nanofiber membrane and depositing active hydroxyapatite onto the fiber membrane, thereby obtaining. The composite fiber membrane has the advantages of favorable combination properties and convenient operation, can effectively promote the capabilities of adherence, growth and calcification osteogenesis of osteoblasts and stem cells, and is hopeful to become an ideal active bracket for bone repair.
Owner:无锡贝迪生物工程股份有限公司

Preparation method of hydroxyapatite/polylactic acid composite coating on surface of medical magnesium alloy

The invention relates to a preparation method of a hydroxyapatite/polylactic acid composite coating on the surface of medical magnesium alloy, which comprises the following steps of polishing a magnesium alloy basal body to remove an oxidation layer on the surface; carrying out acid etching pretreatment and neutralizing treatment on the magnesium alloy basal body; preparing transfer solution from sodium dihydrogen phosphate dihydrate and calcium nitrate terahydrate; preparing a biomimetic calcium-phosphate coating; dissolving polylactic acid in a chloroform solvent to prepare polylactic acid solution; immersing the prepared magnesium alloy/hydroxyapatite composite material in the polylactic acid solution, and coating the polylactic acid coating on the surface of the magnesium alloy/hydroxyapatite composite material by adopting the solution dip-coating method; and putting the magnesium alloy material for 2-3 days till chloroform in the polylactic acid solution is completely volatilized, thereby obtaining the composite material of which the surface of magnesium alloy is wrapped with the hydroxyapatite/polylactic acid composite coating. Compared with the prior art, the preparation method of the hydroxyapatite/polylactic acid composite coating on the surface of medical magnesium alloy overcomes the disadvantages of the single coating, and therefore, the corrosion resistance and the biocompatibility of magnesium alloy are obviously increased.
Owner:TONGJI UNIV

PLGA/Hydroxyapatite Composite Biomaterial and Method of Making the Same

InactiveUS20090048358A1Fastly and highly and uniformly coatedGood at propagatingCosmetic preparationsImpression capsDiseaseApatite
Tissue engineering is a growing field where new materials are being developed for implantation into the body. One important area involves bone graft materials to replace areas of bone lost to trauma or disease. Traditionally, graft material may be harvested from the bone of the individual receiving the graft material. However, this requires an additional surgery and additional recovery. Bone also may be taken from others, or even cadavers, but this introduces biocompatibility problems as well as the risk of disease transfer. Ideally, a biocompatible material is sought that will act as a filler with appropriate mechanical strength, encourage bone healing, and degrade to allow new bone ingrowth without the risk of disease transfer. The present invention is a new composite bone graft material made from biocompatible poly(D,L-lactic-co-glycolic acid) (PLGA) and nano-sized hydroxyapatite particles exposed on its surface using a gas foaming particle leaching (GF / PL) method. A further embodiment of this invention involves coating this PLGA / hydroxyapatite biomaterial with an adherent, fast, uniform coating of a mineral such as apatite. The PLGA polymer portion of the composite provides sufficient mechanical strength to replace bone and is degradable over time to allow new bone tissue ingrowth. The incorporated hydroxyapatite particles increase the composite material's osteogenic properties by providing sites for tissue attachment and propagation. Finally, a uniform coating of mineral apatite on the surface of this novel biomaterial composite further enhances its osteogenic qualities.
Owner:NANO ORTHOPEDICS

PLGA/hydroxyapatite composite biomaterial and method of making the same

InactiveUS20080065228A1Fastly and highly and uniformly coatedGood at propagatingCosmetic preparationsBone implantApatiteBiocompatibility Testing
Tissue engineering is a growing field where new materials are being developed for implantation into the body. One important area involves bone graft materials to replace areas of bone lost to trauma or disease. Traditionally, graft material may be harvested from the bone of the individual receiving the graft material. However, this requires an additional surgery and additional recovery. Bone also may be taken from others, or even cadavers, but this introduces biocompatibility problems as well as the risk of disease transfer. Ideally, a biocompatible material is sought that will act as a filler with appropriate mechanical strength, encourage bone healing, and degrade to allow new bone ingrowth without the risk of disease transfer. The present invention is a new composite bone graft material made from biocompatible poly(D,L-lactic-co-glycolic acid) (PLGA) and nano-sized hydroxyapatite particles exposed on its surface using a gas foaming particle leaching (GF / PL) method. A further embodiment of this invention involves coating this PLGA / hydroxyapatite biomaterial with an adherent, fast, uniform coating of a mineral such as apatite. The PLGA polymer portion of the composite provides sufficient mechanical strength to replace bone and is degradable over time to allow new bone tissue ingrowth. The incorporated hydroxyapatite particles increase the composite material's osteogenic properties by providing sites for tissue attachment and propagation. Finally, a uniform coating of mineral apatite on the surface of this novel biomaterial composite further enhances its osteogenic qualities.
Owner:NANO ORTHOPEDICS

Production method of attapulgite loaded hydroxyapatite composite defluorination filter bulb

The invention discloses a production method of an attapulgite loaded hydroxyapatite composite defluorination filter bulb, which comprises the following steps: preparing attapulgite loaded hydroxyapatite powder from industrial-grade calcium hydroxide, phosphoric acid, acetic acid and attapulgite as raw materials, regulating the solubility of calcium hydroxide using acetic acid, and controlling calcium-phosphorus ratio and pH value of the solution so as to ensure the purity and the defluorination capacity of the products; and fabricating the attapulgite loaded hydroxyapatite powder into pelletsof diameters 0.5-1.5mm, and drying and molding the pellets at a temperature ranging from 350 to 450 DEG C so as to obtain attapulgite loaded hydroxyapatite composite defluorination filter bulb. The composition of attapulgite and hydroxyapatite reduces cost, is helpful for pellet formation, and enhances defluorination of hydroxyapatite. The method of the invention uses cheap and easily-accessible raw materials, high capacity of defluorination filter bulbs, long service life and small fluent water resistance, , and is simple in preparation, easy for control and regeneration, and easy for large-scale industrial production and promotion.
Owner:JIANGSU YONGGUAN WATER & WASTERWATER EQUIP CO LTD +1

Flame-retardant microcrystalline cellulose/hydroxyapatite composite aerogel and preparation method thereof

The invention provides flame-retardant microcrystalline cellulose/hydroxyapatite composite aerogel and a preparation method thereof, relating to the fields of composite aerogel and a preparation method thereof. The preparation method comprises the steps of firstly synthesizing hydroxyapatite nanorods by virtue of a hydrothermal method, dispersing the hydroxyapatite nanorods into deionized water soas to prepare hydroxyapatite dispersion liquid, preparing a microcrystalline cellulose solution by taking a sodium hydroxide/urea water solution as a solvent and epoxy chloropropane as a cross-linking agent, finally, preparing flame-retardant microcrystalline cellulose/hydroxyapatite composite aerogel with a honeycomb structure by virtue of the cooperation of a solution blending method and a vacuum freeze drying method, wherein the hydroxyapatite nanorods with the diameters of 1nm-100nm and the lengths of 10nm-300nm are uniformly dispersed into a microcrystalline cellulose matrix. The prepared composite aerogel has obvious flame retardant effect and smoke release inhibition effect, the safety of aerogel in the fire is remarkably improved, and the adopted microcrystalline cellulose and hydroxyapatite have excellent biocompatibility and environmental friendliness.
Owner:HEFEI UNIV

Polyvinyl alcohol/sodium alginate/hydroxyapatite composite fiber membrane as well as preparation method and application of polyvinyl alcohol/sodium alginate/hydroxyapatite composite fiber membrane

The invention relates to a polyvinyl alcohol / sodium alginate / hydroxyapatite composite fiber membrane as well as a preparation method and application of the polyvinyl alcohol / sodium alginate / hydroxyapatite composite fiber membrane. The preparation method of the composite fiber membrane comprises the following steps: firstly, taking diammonium phosphate and calcium nitrate to react to prepare hydroxyapatite; carrying out ultrasonic dispersion on the hydroxyapatite and sodium alginate to form a stable hydroxyapatite suspension solution; secondly, preparing a sodium alginate solution with the mass percent of 2 percent of a polyvinyl alcohol solution with the mass percent of 18 percent by adopting the suspension solution; finally, uniformly mixing the two types of solutions according to a ratio and carrying out electrostatic spinning. According to the preparation method of the composite fiber membrane, the hydroxyapatite is stably and uniformly dispersed into water by combining the sodium alginate with an ultrasonic method under the condition that other substances are not introduced, and the problem that the hydroxyapatite is easy to agglomerate is solved; the biocompatibility of a natural high polymer and a synthesized high polymer and the bioactivity of hydroxyapatite nanoparticles are combined by adopting the electrostatic spinning to successfully prepare the composite fiber membrane capable of being used as repairing dressing of soft tissue injuries.
Owner:WUHAN UNIV OF TECH

Hydroxyapatite nano-complex particle, preparation and uses thereof

The invention relates to hydroxyapatite composite nanoparticles, which comprise hydroxyapatite of which mass friction is 95 to 99.5 percent and cellulose with the mass friction of between 0.5 and 5 percent, wherein the appearance of the hydroxyapatite composite nanoparticles is a needle of which the length is between 50 and 310 nanometers and the width is between 3 and 30 nanometers. A method for preparing the hydroxyapatite composite nanoparticles comprises the following technological steps: (1) taking a metallic soluble salt aqueous solution or an ammonium salt aqueous solution as a solvent to dissolve the cellulose at a temperature of between 60 and 100 DEG C; (2) adding a calcium salt aqueous solution and a phosphate aqueous solution into a cellulose-salt solution after the cellulose-salt solution prepared in the step (1) is cooled to the room temperature, controlling the mol ratio of Ca to P of a reaction system is 1.2-2.0:1, subsequently adjusting the pH value of the reaction system, stopping stirring when the pH value is stably between 10 and 12, and keeping the obtained solution stand and performing aging for at least 48 hours; and (3) collecting and drying products. The composite particles have stable dispersity in an aqueous-phase medium, and can be taken as a fluorescent molecular carrier.
Owner:SICHUAN UNIV

Method for surface modification of dental implant

The invention mainly discloses a method for surface modification of a metal titanium dental implant. A titanium dioxide/hydroxyapatite composite coating with biocompatibility and biological activity is prepared on the surface of the dental implant by using a multi-electrode method; and the technology is suitable for modifying most of medical metal surfaces. The method mainly comprises the following steps of: (1) ultrasonically cleaning a mechanical face threaded titanium dental implant through ultrapure water, acetone and absolute ethyl alcohol and then drying; (2) uniformly arranging and distributing a titanium dioxide nanotube array with consistent aperture size on an anodic oxide layer of the implant as a buffer layer by using the multi-electrode method; (3) electrodepositing the hydroxyapatite coating in a calcium phosphate electric deposition solution by using the multi-electrode method to prepare the prepared hydroxyapatite coating which is uniformly distributed and has high purity and better biological activity; and (4) processing the material obtained by the process through high-temperature vacuum sintering. The titanium dioxide/hydroxyapatite composite coating prepared by the steps has better bonding strength and superior biological activity, so that the dental implant subjected to surface modification has a broader and longer-range application prospect.
Owner:UNIV OF ELECTRONICS SCI & TECH OF CHINA

Electrodeposition preparation method for biomedical titanium base hydroxyapatite composite material

The present invention discloses a preparation method for electrodeposition of a hydroxyapatite coating on the surface of titanium or a titanium alloy. The method comprises: adopting a pretreated titanium substrate or a pretreated titanium alloy substrate as a cathode, adopting a platinum-plated titanium mesh as an anode, heating an electroplating solution to a constant temperature of 40-80 DEG C, and adopting a constant current manner or a constant potential manner under a magnetic stirring condition to carry out electrodeposition, wherein a current density is 1.0-50.0 mA.cm<-2>, a deposition potential is 1.0-10.0 V, the electroplating solution comprises 20.2-80.0 mmol.L<-1> of Ca<2+> and 10.0-50.0 mmol.L<-1> of H2PO4<->, a Ca/P molar ratio is 1.6-2.0, a supporting electrolyte concentration is 0.1-1.0 mol.L<-1>, and the pH value is 4.2-5.0. According to the present invention, the hydroxyapatite coating prepared through electrodeposition by using the constant current manner or the constant potential manner has characteristics of fine crystal, smooth surface, strong bonding force with the substrate, good biological activity and mechanical property. The preparation method for the titanium base hydroxyapatite composite material has characteristics of mild reaction condition, avoidance of influence on material biological activity by a high temperature treatment, simple process, and low equipment investment, wherein a series of problems caused by expensive equipment and complex operation of the existing method are overcome with the preparation method.
Owner:TIANJIN XUANZHEN BIOMEDICAL TECH DEV
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